Canonical Allele Identifier: CA443535659

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13770995C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770886C>A , CM000667.2:g.13770886C>A	GRCh38
NC_000005.9:g.13770995C>A , CM000667.1:g.13770995C>A	GRCh37
NC_000005.8:g.13823995C>A	NCBI36
NG_013081.1:g.178595G>T
NG_013081.2:g.178595G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9468G>T MANE Select	ENSP00000265104.4:p.Val3156=
ENST00000681290.1:c.9423G>T	ENSP00000505288.1:p.Val3141=
ENST00000265104.4:c.9468G>T	ENSP00000265104.4:p.Val3156=
ENST00000504001.3:n.180G>T
NM_001369.2:c.9468G>T	NP_001360.1:p.Val3156=
XM_005248262.2:c.9423G>T	XP_005248319.1:p.Val3141=
XM_005248262.3:c.9576G>T	XP_005248319.2:p.Val3192=
XM_017009177.1:c.9576G>T	XP_016864666.1:p.Val3192=
XM_017009178.1:c.8481G>T	XP_016864667.1:p.Val2827=
XM_017009179.2:c.8481G>T	XP_016864668.1:p.Val2827=
XM_017009180.1:c.9576G>T	XP_016864669.1:p.Val3192=
XM_017009181.1:c.9576G>T	XP_016864670.1:p.Val3192=
XM_017009182.1:c.9576G>T	XP_016864671.1:p.Val3192=
XM_017009183.1:c.9576G>T	XP_016864672.1:p.Val3192=
XM_017009185.1:c.4665G>T	XP_016864674.1:p.Val1555=
XM_017009186.1:c.4218G>T	XP_016864675.1:p.Val1406=
XM_017009188.1:c.3555G>T	XP_016864677.1:p.Val1185=
XM_024454388.1:c.8481G>T	XP_024310156.1:p.Val2827=
XM_024454389.1:c.8070G>T	XP_024310157.1:p.Val2690=
NM_001369.3:c.9468G>T MANE Select	NP_001360.1:p.Val3156=